![Further case of microdeletion of 8q24 with phenotype overlapping Langer– Giedion without TRPS1 deletion - McBrien - 2008 - American Journal of Medical Genetics Part A - Wiley Online Library Further case of microdeletion of 8q24 with phenotype overlapping Langer– Giedion without TRPS1 deletion - McBrien - 2008 - American Journal of Medical Genetics Part A - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/b398537a-4eb2-4df5-8dfe-b275f531b0b2/mfig002.jpg)
Further case of microdeletion of 8q24 with phenotype overlapping Langer– Giedion without TRPS1 deletion - McBrien - 2008 - American Journal of Medical Genetics Part A - Wiley Online Library
![Long‐term follow‐up of four patients with langer–giedion syndrome: Clinical course and complications - Schinzel - 2013 - American Journal of Medical Genetics Part A - Wiley Online Library Long‐term follow‐up of four patients with langer–giedion syndrome: Clinical course and complications - Schinzel - 2013 - American Journal of Medical Genetics Part A - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/85e5b6aa-758f-4781-a93e-4fad7cfc6b70/ajmga36062-fig-0003-m.jpg)
Long‐term follow‐up of four patients with langer–giedion syndrome: Clinical course and complications - Schinzel - 2013 - American Journal of Medical Genetics Part A - Wiley Online Library
![An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature | Italian Journal of Pediatrics | Full Text An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature | Italian Journal of Pediatrics | Full Text](https://media.springernature.com/m685/springer-static/image/art%3A10.1186%2Fs13052-018-0580-z/MediaObjects/13052_2018_580_Fig2_HTML.png)
An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature | Italian Journal of Pediatrics | Full Text
![Tetraparesis due to exostotic osteochondroma at upper cervical cord in a patient with multiple exostoses–mental retardation syndrome (Langer–Giedion syndrome) | Spinal Cord Tetraparesis due to exostotic osteochondroma at upper cervical cord in a patient with multiple exostoses–mental retardation syndrome (Langer–Giedion syndrome) | Spinal Cord](https://media.springernature.com/full/springer-static/image/art%3A10.1038%2Fsj.sc.3101690/MediaObjects/41393_2005_Article_BF3101690_Fig1_HTML.jpg)
Tetraparesis due to exostotic osteochondroma at upper cervical cord in a patient with multiple exostoses–mental retardation syndrome (Langer–Giedion syndrome) | Spinal Cord
![An interstitial deletion at 8q23.1-q24.12 associated with Langer-Giedion syndrome/ Trichorhinophalangeal syndrome (TRPS) type II and Cornelia de Lange syndrome 4 | Molecular Cytogenetics | Full Text An interstitial deletion at 8q23.1-q24.12 associated with Langer-Giedion syndrome/ Trichorhinophalangeal syndrome (TRPS) type II and Cornelia de Lange syndrome 4 | Molecular Cytogenetics | Full Text](https://media.springernature.com/full/springer-static/image/art%3A10.1186%2Fs13039-015-0169-9/MediaObjects/13039_2015_169_Fig1_HTML.gif)
An interstitial deletion at 8q23.1-q24.12 associated with Langer-Giedion syndrome/ Trichorhinophalangeal syndrome (TRPS) type II and Cornelia de Lange syndrome 4 | Molecular Cytogenetics | Full Text
Nationwide Children's Hospital - Mile 10 - Kolby Langer Giedion Syndrome Find out how you can help support kids like Kolby: http://goo.gl/bu1RmO | Facebook
![Patient at 4 years of age. Note bushy eyebrows, synophrys, esotropia at... | Download Scientific Diagram Patient at 4 years of age. Note bushy eyebrows, synophrys, esotropia at... | Download Scientific Diagram](https://www.researchgate.net/publication/259395257/figure/fig2/AS:267622264602635@1440817528077/Patient-at-4-years-of-age-Note-bushy-eyebrows-synophrys-esotropia-at-left-eye-long.png)
Patient at 4 years of age. Note bushy eyebrows, synophrys, esotropia at... | Download Scientific Diagram
![Aos 50 anos, escritor que tem síndrome rara busca outros casos de Langer- Giedion na internet | Minas Gerais | G1 Aos 50 anos, escritor que tem síndrome rara busca outros casos de Langer- Giedion na internet | Minas Gerais | G1](https://s2-g1.glbimg.com/uf19hGoGCr1yGpm-uH6qhWn3hv4=/0x0:1700x1065/984x0/smart/filters:strip_icc()/i.s3.glbimg.com/v1/AUTH_59edd422c0c84a879bd37670ae4f538a/internal_photos/bs/2019/A/k/K734leTtmwcUPdUoI0rQ/whatsapp-image-2019-06-12-at-173.jpg)
Aos 50 anos, escritor que tem síndrome rara busca outros casos de Langer- Giedion na internet | Minas Gerais | G1
Síndrome de Langer-Giedion con deleción 8q23.1-q24.12, diagnosticado por hibridación genómica comparativa
![Prenatal diagnosis and array comparative genomic hybridization characterization of interstitial deletions of 8q23.3–q24.11 and 8q24.13 associated with Langer-Giedion syndrome, Cornelia de Lange syndrome and haploinsufficiency of TRPS1, RAD21 and EXT1 ... Prenatal diagnosis and array comparative genomic hybridization characterization of interstitial deletions of 8q23.3–q24.11 and 8q24.13 associated with Langer-Giedion syndrome, Cornelia de Lange syndrome and haploinsufficiency of TRPS1, RAD21 and EXT1 ...](https://ars.els-cdn.com/content/image/1-s2.0-S1028455915001710-gr3.jpg)